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 DeCS Categories

C04 Neoplasms .
C04.557 Neoplasms by Histologic Type .
C04.557.450 Neoplasms, Connective and Soft Tissue .
C04.557.450.565 Neoplasms, Connective Tissue .
C04.557.450.565.550 Myxoma .
C04.557.450.565.550.312 Carney Complex .
C04.588 Neoplasms by Site .
C04.588.894 Thoracic Neoplasms .
C04.588.894.309 Heart Neoplasms .
C04.588.894.309.500 Carney Complex .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.425 Lesch-Nyhan Syndrome .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.643 Intellectual Disability .
C10.597.606.643.455 Mental Retardation, X-Linked .
C10.597.606.643.455.625 Lesch-Nyhan Syndrome .
C14 Cardiovascular Diseases .
C14.280 Heart Diseases .
C14.280.459 Heart Neoplasms .
C14.280.459.500 Carney Complex .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.229 Carney Complex .
C16.131.831 Skin Abnormalities .
C16.131.831.108 Carney Complex .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.500 Mental Retardation, X-Linked .
C16.320.322.500.625 Lesch-Nyhan Syndrome .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.525 Mental Retardation, X-Linked .
C16.320.400.525.625 Lesch-Nyhan Syndrome .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.425 Lesch-Nyhan Syndrome .
C16.320.565.798 Purine-Pyrimidine Metabolism, Inborn Errors .
C16.320.565.798.594 Lesch-Nyhan Syndrome .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.463 Lipomatosis .
C17.800.463.249 Adiposis Dolorosa .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.425 Lesch-Nyhan Syndrome .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.718 Lipomatosis .
C18.452.584.718.500 Adiposis Dolorosa .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.425 Lesch-Nyhan Syndrome .
C18.452.648.798 Purine-Pyrimidine Metabolism, Inborn Errors .
C18.452.648.798.594 Lesch-Nyhan Syndrome .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
C23.550.288.500 Syndrome .
D02 Organic Chemicals .
D02.065 Amides .
D02.065.884 Sulfonamides .
D02.065.884.725 Sulfanilamides .
D02.065.884.725.867 Sulfamethoxazole .
D02.065.884.725.867.500 Trimethoprim, Sulfamethoxazole Drug Combination .
D02.092 Amines .
D02.092.146 Aniline Compounds .
D02.092.146.807 Sulfanilamides .
D02.092.146.807.867 Sulfamethoxazole .
D02.092.146.807.867.500 Trimethoprim, Sulfamethoxazole Drug Combination .
D02.886 Sulfur Compounds .
D02.886.590 Sulfones .
D02.886.590.700 Sulfonamides .
D02.886.590.700.725 Sulfanilamides .
D02.886.590.700.725.867 Sulfamethoxazole .
D02.886.590.700.725.867.500 Trimethoprim, Sulfamethoxazole Drug Combination .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.742 Pyrimidines .
D03.383.742.906 Trimethoprim .
D03.383.742.906.500 Trimethoprim, Sulfamethoxazole Drug Combination .
D26 Pharmaceutical Preparations .
D26.310 Drug Combinations .
D26.310.875 Trimethoprim, Sulfamethoxazole Drug Combination .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Lesch-Nyhan Syndrome .
Choreoathetosis Self-Mutilation Syndrome .
Complete HGPRT Deficiency Disease .
Complete HPRT Deficiency .
Complete Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency .
Deficiency Disease, Complete HGPRT .
Deficiency Disease, Hypoxanthine-Phosphoribosyl-Transferase .
Deficiency of Guanine Phosphoribosyltransferase .
Deficiency of Hypoxanthine Phosphoribosyltransferase .
HGPRT Deficiency .
HGPRT Deficiency Disease, Complete .
Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency .
Hypoxanthine Guanine Phosphoribosyltransferase Deficiency .
Hypoxanthine Phosphoribosyltransferase Deficiency .
Juvenile Gout, Choreoathetosis, Mental Retardation Syndrome .
Juvenile Hyperuricemia Syndrome .
Lesch-Nyhan Disease .
Primary Hyperuricemia Syndrome .
Total HPRT Deficiency .
Total Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency .
X-Linked Hyperuricemia .
X-Linked Primary Hyperuricemia .
Choreoathetosis Self Mutilation Hyperuricemia Syndrome .
Choreoathetosis Self Mutilation Syndrome .
Choreoathetosis Self-Mutilation Syndromes .
Complete HPRT Deficiencies .
Complete Hypoxanthine Guanine Phosphoribosyltransferase Deficiency .
Deficiencies, Complete HPRT .
Deficiencies, HGPRT .
Deficiencies, Hypoxanthine Phosphoribosyltransferase .
Deficiencies, Total HPRT .
Deficiency Disease, Hypoxanthine Phosphoribosyl Transferase .
Deficiency Diseases, Hypoxanthine-Phosphoribosyl-Transferase .
Deficiency, Complete HPRT .
Deficiency, HGPRT .
Deficiency, Hypoxanthine Phosphoribosyltransferase .
Deficiency, Total HPRT .
Guanine Phosphoribosyltransferase Deficiencies .
Guanine Phosphoribosyltransferase Deficiency .
HGPRT Deficiencies .
HPRT Deficiencies, Complete .
HPRT Deficiencies, Total .
HPRT Deficiency, Complete .
HPRT Deficiency, Total .
Hyperuricemia Syndrome, Juvenile .
Hyperuricemia Syndrome, Primary .
Hyperuricemia Syndromes, Juvenile .
Hyperuricemia Syndromes, Primary .
Hyperuricemia, X-Linked .
Hyperuricemia, X-Linked Primary .
Hyperuricemias, X-Linked .
Hyperuricemias, X-Linked Primary .
Hypoxanthine Phosphoribosyl Transferase Deficiency Disease .
Hypoxanthine Phosphoribosyltransferase Deficiencies .
Hypoxanthine-Phosphoribosyl-Transferase Deficiency Diseases .
Juvenile Hyperuricemia Syndromes .
Lesch Nyhan Disease .
Lesch Nyhan Syndrome .
Phosphoribosyltransferase Deficiencies, Guanine .
Phosphoribosyltransferase Deficiencies, Hypoxanthine .
Phosphoribosyltransferase Deficiency, Guanine .
Phosphoribosyltransferase Deficiency, Hypoxanthine .
Primary Hyperuricemia Syndromes .
Primary Hyperuricemia, X-Linked .
Primary Hyperuricemias, X-Linked .
Self-Mutilation Syndrome, Choreoathetosis .
Self-Mutilation Syndromes, Choreoathetosis .
Syndrome, Choreoathetosis Self-Mutilation .
Syndrome, Juvenile Hyperuricemia .
Syndrome, Primary Hyperuricemia .
Syndromes, Choreoathetosis Self-Mutilation .
Syndromes, Juvenile Hyperuricemia .
Syndromes, Primary Hyperuricemia .
Total HPRT Deficiencies .
Total Hypoxanthine Guanine Phosphoribosyl Transferase Deficiency .
X Linked Hyperuricemia .
X Linked Primary Hyperuricemia .
X-Linked Hyperuricemias .
X-Linked Primary Hyperuricemias .
Choreoathetosis Self-Mutilation Hyperuricemia Syndrome .
Hypoxanthine-Phosphoribosyl-Transferase Deficiency Disease .
An inherited disorder transmitted as a sex-linked trait and caused by a deficiency of an enzyme of purine metabolism; HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE. Affected individuals are normal in the first year of life and then develop psychomotor retardation, extrapyramidal movement disorders, progressive spasticity, and seizures. Self-destructive behaviors such as biting of fingers and lips are seen frequently. Intellectual impairment may also occur but is typically not severe. Elevation of uric acid in the serum leads to the development of renal calculi and gouty arthritis. (Menkes, Textbook of Child Neurology, 5th ed, pp127) .
1.00
201179
 
Syndrome .
Symptom Cluster .
Cluster, Symptom .
Clusters, Symptom .
Symptom Clusters .
Syndromes .
A characteristic symptom complex. .
0.49
1572102931
 
Carney Complex .
Carney Complex, Type 1 .
Carney Complex, Type I .
Carney Myxoma-Endocrine Complex, Type II .
LAMB - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome .
Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome .
Carney Myxoma Endocrine Complex .
Carney Myxoma Endocrine Complex, Type II .
Complex, Carney .
Complex, Carney Myxoma-Endocrine .
LAMB Syndromes .
Myxoma-Endocrine Complex, Carney .
NAME Syndromes .
Syndrome, Carney .
Syndrome, LAMB .
Syndromes, LAMB .
Carney Complex, Type 2 .
Carney Complex, Type II .
Carney Myxoma-Endocrine Complex .
Carney Syndrome .
LAMB Syndrome .
Myxoma, Spotty Pigmentation, and Endocrine Overactivity .
NAME Syndrome .
Autosomal dominant syndrome characterized by cardiac and cutaneous MYXOMAS; LENTIGINOSIS (spotty pigmentation of the skin), and endocrinopathy and its associated endocrine tumors. The cardiac myxomas may lead to SUDDEN CARDIAC DEATH and other complications in Carney complex patients. The gene coding for the PRKAR1A protein is one of the causative genetic loci (type 1). A second locus is at chromosome 2p16 (type 2). .
0.41
12154
 
Trimethoprim, Sulfamethoxazole Drug Combination .
Abactrim .
Bactifor .
Bactrim .
Biseptol .
Biseptol-480 .
Centran .
Centrin .
Co-Trimoxazole .
Cotrimoxazole .
Drylin .
Eslectin .
Eusaprim .
Insozalin .
Kepinol .
Kepinol Forte .
Lescot .
Metomide .
Oriprim .
Septra .
Septrin .
Sulfamethoxazole-Trimethoprim Combination .
Sulprim .
Sumetrolim .
TMP SMX .
TMP-SMX .
Trimedin .
Trimethoprim-Sulfamethoxazole .
Trimethoprimsulfa .
Trimezole .
Trimosulfa .
Biseptol 480 .
Biseptol480 .
Co Trimoxazole .
Sulfamethoxazole Trimethoprim Combination .
Trimethoprim Sulfamethoxazole .
Trimethoprim Sulfamethoxazole Combination .
Cotrimoxazole .
Trimethoprim-Sulfamethoxazole Combination .
Trimethoprim, Sulfamethoxazole Combination .
A drug combination with broad-spectrum antibacterial activity against both gram-positive and gram-negative organisms. It is effective in the treatment of many infections, including PNEUMOCYSTIS PNEUMONIA in AIDS. .
0.39
2376387
 
Adiposis Dolorosa .
Adiposalgia .
Adipose Tissue Rheumatism .
Ander's Syndrome .
Anders Syndrome .
Decum-Vitaut Syndrome .
Dercum Disease .
Lipomatosis Dolorosa .
Morbus Dercum .
Adiposalgias .
Adipose Tissue Rheumatisms .
Ander Syndrome .
Anders Syndromes .
Decum Vitaut Syndrome .
Dercum, Morbus .
Dercums Disease .
Dercums, Morbus .
Disease, Dercum .
Disease, Dercum's .
Dolorosa, Lipomatosis .
Dolorosas, Lipomatosis .
Lipomatosis Dolorosas .
Morbus Dercums .
Rheumatism, Adipose Tissue .
Rheumatisms, Adipose Tissue .
Syndrome, Ander's .
Syndrome, Anders .
Syndrome, Decum-Vitaut .
Syndromes, Anders .
Tissue Rheumatism, Adipose .
Tissue Rheumatisms, Adipose .
Dercum's Disease .
A rare disease characterized by multiple tumor-like fatty deposits that press on nerves in various sites causing pain and weakness. Often these lipoma-like structures are located on the trunk and limbs but not on the face and hands. .
0.37
7119